Delizza BELGIAN MINI CHOCOLATE CREAM PUFFS NET WT. 14.1 oz (400g) 30 CREAM PUFFS PRODUCED IN THE US BY DELIZZA INCORPORA
Summary
The FDA issued a Class II for Delizza BELGIAN MINI CHOCOLATE CREAM PUFFS NET WT. 14.1 oz (400g) 30 CREAM PUFFS by Poppies International INC. Reason: The firm found small pieces of metal in the bakery palm oil silo which were not able to be detected every pass through the metal detector..
Details
Source
Food Recall
External ID
F-0627-2022
Action Date
2022-02-09
Status
Ongoing
Category
food
Product Description
Delizza BELGIAN MINI CHOCOLATE CREAM PUFFS NET WT. 14.1 oz (400g) 30 CREAM PUFFS PRODUCED IN THE US BY DELIZZA INCORPORATED 6610 CORPORATION PARKWAY, BATTLEBORO, NC 27809 UPC 6 76670 00402 2
Lot/Code Info: L1J5021, BEST BEFORE 06/09/23 & L1K5021 BEST BEFORE 06/09/23
Quantity Affected: 2,052 cs/6/30 Cream Puffs
Reason for Recall
The firm found small pieces of metal in the bakery palm oil silo which were not able to be detected every pass through the metal detector.
Distribution
Product was shipped to the following states: CA, NY, PA, WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-23
Company
Battleboro, NC
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 112 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Poppies International INC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Poppies International INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Poppies International INC have FDA actions?
Poppies International INC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0627-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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